Henoch-Schonlein purpura associated with segmental and focal proliferative glomerulonephritis in a patient with Hodgkin's disease

Blanco, Paula; Denisi, R; Rispal, P; Déminière, C.; Pellegrin, JL; Li, Bing; Aparicio, M

doi:10.1093/ndt/14.1.179

Cited by 24 publications

(10 citation statements)

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“…Renal carcinoma has been associated with Wegener's granulomatosis (WG) and may precipitate the onset of WG [10]. There are further case reports and a small series suggesting a link between malignancy and Henoch-Scho¨nlein purpura (HSP) [6,[12][13][14][15][16][17]. Most of these reports link HSP with solid organ tumours, but haematological malignancy has also been reported.…”

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confidence: 99%

Malignancy is increased in ANCA-associated vasculitis

et al. 2004

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confidence: 99%

Malignancy is increased in ANCA-associated vasculitis

et al. 2004

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“…13 There have been several reports about cutaneous vasculitis associated with hematological malignancies including T-cell lymphoma. [14][15][16] On the other hand, most (63%) of the malignant neoplasms associated with adult HSP were solid tumors, as reported by Pertuiset et al 12 Many of hematologic malignancies that are associated with HSP are composed of B cells, such as Hodgkin's disease, 17,18 non-Hodgkin's B-cell lymphoma, 19,20 and multiple myeloma, 21-23 which may suggest a relationship of IgA increase in these diseases to the production of IgA containing immune complexes, which can cause vasculitis of small vessels in HSP.…”

Section: Discussionmentioning

confidence: 99%

Adult T-cell lymphoma mimicking Henoch–Schönlein purpura

Tabata

Namiuchi

et al. 2007

Mod Rheumatol

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We report a male patient with adult T-cell lymphoma, who was initially diagnosed clinically as having Henoch-Schönlein purpura (HSP) with abdominal pain and specific purpura. Adult T-cell lymphoma-like cells were minimal and abdominal lymph nodes were transiently swollen, and the symptoms were improved by supportive management. Although the clinical course was compatible with HSP, the histological examination revealed infiltration of lymphocytes rather than neutrophils. Later he developed lymphoma and was treated with chemotherapy. This rare case suggests the importance of skin biopsies to seek the underlying pathology in adult HSP.

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“…Blanco et al [7] reported a 29-year-old male who presented with fever, night sweating, cervical mass and typical symptoms of HSP. Skin biopsy showed leukocytoclastic vasculitis without any immunofluorescence deposit.…”

Section: Urinary Proteome Analysismentioning

confidence: 99%

“…Secondary IgAN is associated with several diseases, including immunological disorders, infections and cancers. Malignancies that have been reported to be associated with IgAN include renal cell carcinoma [2], cancers of the lung [3], larynx [4] and esophagus [5], cutaneous T-cell lymphoma [6], Hodgkin's disease [7][8][9], and non-Hodgkin lymphoma [10]. Secondary IgAN in patients with Hodgkin's lymphoma is very rare, and its pathogenic mechanisms remain unclear.…”

Section: Introductionmentioning

confidence: 99%

IgA nephropathy associated with Hodgkin’s disease in children: a case report, literature review and urinary proteome analysis

et al. 2007

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We report herein a rare case of IgAN associated with Hodgkin's disease in a 14-year-old boy. Clinical manifestations and laboratory parameters were improved after treatment with CHOP chemotherapy and enalapril. Urinary proteins were isolated and examined using state-of-the-art proteomic technology, before and during the treatment course. Two-dimensional gel electrophoresis showed obvious alterations in the urinary proteome profile in response to such therapy. Quantitative intensity analysis and gel mapping revealed 14 altered proteins with reduced excretion levels during the treatment course, including albumin, albumin complexed with decanoic acid, alpha-1 antitrypsin, cadherin-11 precursor, collagen alpha 1 (VI) chain precursor, complement C1q tumor necrosis factor-related protein, Ig heavy chain, Ig light chain, kininogen, inter-alpha-trypsin inhibitor (alpha-1 microglobulin), inter-alpha-trypsin inhibitor heavy chain, leucine-rich alpha-2 glycoprotein, beta-2 microglobulin, and transferrin precursor. Their potential roles in the pathogenesis and pathophysiology of IgAN are discussed.

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Henoch-Schonlein purpura associated with segmental and focal proliferative glomerulonephritis in a patient with Hodgkin's disease

Cited by 24 publications

References 0 publications

Malignancy is increased in ANCA-associated vasculitis

Malignancy is increased in ANCA-associated vasculitis

Adult T-cell lymphoma mimicking Henoch–Schönlein purpura

IgA nephropathy associated with Hodgkin’s disease in children: a case report, literature review and urinary proteome analysis

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